National Urea Cycle Disorders Foundation
Non-profit Organizations
Pasadena, California 489 followers
Dedicated to saving and improving the lives of children and adults with urea cycle disorders.
About us
We know Urea Cycle Disorders. We live to conquer them. The National Urea Cycle Disorders Foundation is the only nonprofit organization in the world solely dedicated to saving and improving the lives of children and adults from the catastrophic effects of urea cycle disorders. Formed in 1988 by a handful of parents whose children were affected, NUCDF has grown to be an internationally recognized leader in the fight to conquer urea cycle disorders (UCD) and raise awareness that saves lives. NUCDF is the driving force behind critical research to improve the understanding and management of UCD, find new treatments, and ultimately a cure. NUCDF serves as a lifeline to UCD patients, families, and medical professionals worldwide seeking information, support, and HOPE. We partner with the Urea Cycle Disorders Consortium, an NIH-funded Rare Diseases Clinical Research Network, to advance research in this area.
- Website
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http://nucdf.org
External link for National Urea Cycle Disorders Foundation
- Industry
- Non-profit Organizations
- Company size
- 2-10 employees
- Headquarters
- Pasadena, California
- Type
- Nonprofit
- Founded
- 1988
- Specialties
- Rare diseases, Patient advocacy, Medical research, Urea cycle disorders, Community building, Education, Public awareness, Ornithine Transcarbamylase (OTC) Deficiency, Carbamoyl-phosphate Synthase 1 (CPS1) Deficiency, Argininosuccinate lyase deficiency (ASLD), argininosuccinic aciduria, citrullinemia, Argininosuccinate Synthase (ASS) Deficiency, hyperargininemia, N-acetylglutamate Synthase (NAGS) Deficiency, citrin deficiency, hyperammonemia, and Arginase (ARG) Deficiency
Locations
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Primary
Get directions
75 S Grand Ave
Pasadena, California 91105, US
Employees at National Urea Cycle Disorders Foundation
Updates
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Happy Halloween to those who celebrate! #happyhalloween #halloween
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National Urea Cycle Disorders Foundation reposted this
Essential steps for an accurate plasma ammonia test. #checkammonia #bloodammonia #hyperammonemia #ureacycle #ureacycledisorders
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Essential steps for an accurate plasma ammonia test. #checkammonia #bloodammonia #hyperammonemia #ureacycle #ureacycledisorders
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Here are the proper procedures for an accurate plasma ammonia test. #checkammonia #bloodammonia #ureacycledisorder #ureacycledisorders #rarediseases #metabolicdisorders #geneticdisorders #hyperammonemia
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Did you know: Recurring headaches, especially when combined with irritability or confusion, could be early warning signs of high ammonia levels? #checkammonia #highammonialevels #bloodammonia #ureacycledisorders
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National Urea Cycle Disorders Foundation reposted this
Jennings Larue was born on November 7, 2023. After spending 24 hours in the hospital, the healthy baby was released to go home. The first night home, Jennings was fussy and didn’t really have a desire to eat during the night. The next morning he was much fussier and, as the morning went on, his breathing became shallow and labored. He was taken to the hospital, where he was minimally responsive. He was transferred to OU Children’s Hospital, where doctors began an immediate assessment. Results of tests indicated that Jennings had Citrullinemia Type 1, a rare metabolic disorder. With this disorder, protein isn’t broken down, which causes a build-up of nitrogen in the form of ammonia in the blood. Doctors and specialists worked on Jennings for the next 12 hours but were unable to save him. Jennings passed away shortly after 2:00 pm on November 10, 2023. The Newborn Screen Test was performed although the results were too late for Jennings. Read more about Jennings Legacy here https://lnkd.in/eq6CD7Nq #jenningslegacy #checkammonia #hyperammonemia #bloodammonia #ureacycledisorder #ureacycledisorders
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Jennings Larue was born on November 7, 2023. After spending 24 hours in the hospital, the healthy baby was released to go home. The first night home, Jennings was fussy and didn’t really have a desire to eat during the night. The next morning he was much fussier and, as the morning went on, his breathing became shallow and labored. He was taken to the hospital, where he was minimally responsive. He was transferred to OU Children’s Hospital, where doctors began an immediate assessment. Results of tests indicated that Jennings had Citrullinemia Type 1, a rare metabolic disorder. With this disorder, protein isn’t broken down, which causes a build-up of nitrogen in the form of ammonia in the blood. Doctors and specialists worked on Jennings for the next 12 hours but were unable to save him. Jennings passed away shortly after 2:00 pm on November 10, 2023. The Newborn Screen Test was performed although the results were too late for Jennings. Read more about Jennings Legacy here https://lnkd.in/eq6CD7Nq #jenningslegacy #checkammonia #hyperammonemia #bloodammonia #ureacycledisorder #ureacycledisorders
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Did you know: Persistent nausea, vomiting, or loss of appetite could be signs of high ammonia? #symptoms #highammonia #hyperammonemia #bloodammonialevels #ureacycle #ureacycledisorders #inbornerrorsofmetabolism #checkammonia
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Check ammonia immediately in infants, children, or adults with unexplained: GI presentations, alterations in consciousness, encephalopathy, movement disorders or seizures, learning problems or developmental delays, psychiatric presentations. Learn more at checkammonia.com. #checkammonia #bloodammonialevels #hyperammonemia #ureacycle #ureacycledisorder #ureacycledisorders
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